Murderball Reflection

In Nancy Mairs’ article for The New York Times, “Disability”, published in 1987, she expresses her distaste with the media's representation of handicapped people. Mairs, who struggled with multiple sclerosis herself, clearly and sharply conveys this disgust by stating, “I’m not, for instance, Ms. MS, a walking, talking embodiment of a chronic incurable degenerative disease.” (Mairs 13), and that she is actually, “the advertisers’ dream: Ms. Great American Consumer. And yet the advertisers, who determine nowadays who will get represented publicly and who will not, deny the existence of me and my kind absolutely”(Mairs 14). Mairs is greatly upset that disabled people are defined by their disabilities and, therefore, are underrepresented in public media. This might lead to one asking themselves, but why are they? And the answer, according to Mairs, is quite simple, “To depict disabled people in the ordinary activities of daily life is to admit that there is something ordinary about disability itself, that it may enter anybody’s life”(Mairs 14). Mairs concludes by pointing out how this effacement could have dangerous consequences for both disabled people and, as she called everyone else, TAPs (Temporarily Abled Persons) alike. Treating disabilities as an abnormal characteristic (as opposed to viewing them “as a normal characteristic, one that complicates but does not ruin human existence” (Mairs 15)) can cause one of these repercussions, as it makes the

In her essay “On Being a Cripple”, Nancy Mairs presents her audience with an honest inside view of her life and perspective as a cripple, a word she openly uses to define herself. She brings her world to us by discussing a wide variety of things including language, family, and humor, and how these all relate to her life. Through various stories and insights, she allows her readers to gain an understanding and acceptance of people with disabilities. She examines the public’s view of the disabled, as well as the views they have of themselves, and compares them to her own. She makes it clear that she is not to be defined solely by her disability. In discussing honestly her views, as well as

The movie Murderball, is a documentary about the crazy sport called " quad rugby”. This sport can be very dangerous to most of the players since they are Quadriplegia which means most of the players are wheel chair bounded and have partial or total loss of use of all their limbs and torso. That doesn't stop the players who strive for the intensity, and thrill of the game of rugby. The movie goes into detail about how the main characters became quadriplegic, some were born with an illness, other became quadriplegic from horrible accidents. However, their disability does not stop them from striving to be amazing athletes, and pursuing gold medal in the Olympics.

In the book, The Short Bus, Jonathan Mooney’s thesis is that there is more to people than their disabilities, it is not restricting nor is it shameful but infact it is beautiful in its own way. With a plan to travel the United States, Mooney decides to travel in a Short bus with intentions of collecting experiences from people who have overcome--or not overcome--being labeled disabled or abnormal. In this Mooney reinvents this concept that normal people suck; that a simple small message of “you’re not normal” could have a destructive and deteriorating effect. With an idea of what disabilities are, Mooney’s trip gives light to disabilities even he was not prepared to face, that he feared.

The hot headed and brass attitudes of the players and this documentary, does not take the typical approach to disability. Instead it takes a “wondrous” approach, “capitalizing on physical differences in order to elicit amazement and admiration” (Garland-Thomas 545). The viewers gain a feeling of respect and awe for the players because they “inspire the viewer by performing feats that the nondisabled viewer cannot imagine doing” (Garland-Thomas 545). Most people see disability as something that will never be recovered from, but this movie and these men challenge the viewer to see the strength behind

In her essay, “On Being a Cripple”, Nancy Mairs, an essayist with multiple sclerosis, writes about her experiences with her disease. She wants her audience of able-bodied people to stop pitying towards disabled people and instead show acceptance. Mairs achieves her purpose by presenting herself as similar and relatable to her able-bodied audience with many anecdotes and a blunt tone. This discussion of her condition removes the discomfort about disabilities felt by her audience and allows for them to accept disabled people. While Maris’s primary audience is an able-bodied person who supports disabled people, other readers, like someone with her condition, may be drawn towards this essay as well. Unlike an able-bodied person, a disabled person

This essay highlights and discusses models of disability reflected in two separate articles (Appendices A and B). I will identify the models of disability they represent. Both have been recently featured in the Guardian newspaper and are stories on disabled people.

The featured film documentary called ‘Murder Ball’ directed by Dana Ruben and Alex Shapiro focuses on Mark Zupan and Joe Soares life of a Quadriplegic person. I have responded to the main characters and their situations including how they make me feel about the lives of Quadriplegic people and how they deal with it during their lifetime. My overall impressions about Mark Zupan and Joe Soares lives as a quadriplegic has encouraged me to respond not to feel sorry for them but to gain respect and be inspired .I will be discussing the film techniques to support my ideas in the documentary.

Everyone has their own way of achieving victory: scoring the winning point in a sport, getting chosen for a job or acing a test in school. A writer for Sport Illustrated's, Rick Reilly, tells Ben Comen’s story, a teenager with cerebral palsy who runs for his high school’s cross-country team, in his article “Worth the Wait.” In the article, Reilly informs the audience of the previously mentioned situation that Ben is in, while also mentioning Ben’s process of overcoming all odds and managing to finish the races with the entire crowd cheering him on. Reilly establishes a triumphant tone with the aid of pathos and arduous-like diction to make light of people with cerebral palsy and to show how they can accomplish goals in life like everyone else

So, 2015 AEP was no different in the fact that I meant some really exceptional people. I meant a couple and the wife grew up in Costa Rica. This is significant because I want to retire in that region. I meant a lady from Grenda, she made me this bread for Thanksgiving that was delicious. I meant another couple that I can not say enough about because it seems they have lived all over the world and they have these amazing pieces in their home with history and the depth the kind that you have lasting conversations over.

In the media today, people with disabilities are perceived as tragic heroes or as medical miracles. They are rarely seen for their intelligence or for their accomplishments excluding their overcoming disability hardships. The textbook, Everything’s an Argument, contains an excerpt from Charles A. Riley II 's book “Disability and the Media: Prescriptions for Change.” Riley, a journalism professor at New York’s Baruch College, uses appeal to ethos, logos, and pathos to persuade his audience that their methods of portraying disabled people are in dire need of change.

Disability has appeared frequently in recent films (Byrd & Elliot, 1988), a reflection of society’s interest in the subject. These films often misrepresent disability using stereotypes. These stereotypes reinforce negative and incorrect social perceptions of, and attitudes towards,

I am a senior at Belleville West High School in Illinois. I know this a bit informal but I wanted to make sure there was a way you could get my message other than through the NBA website. Our Key Club is going to Fiji in March to help better the community. We have all of our travel plans taken care of, but we need money to cover the expenses. We thought it was a good idea to host a 3v3 tournament to make up for the funds we do not have. It cost $15,000 to pay for all five of us. I know the NBA is one of the most successful basketball franchises, so when we mentioned basketball I thought NBA. I knew it would be a long shot for you to even respond, but from my experience, the worst you could say is no or contribute in another way. I also would

The dominant model of disability for the majority of the 20th century was the medical model. The medical model’s emphasis is on impairment; this is the cause of the disadvantage disabled individuals face and therefore the site of interventions (Crow, 1996). It is based in the biomedical and clinical. It views disability as a personal tragedy, an idea which is often implicit in work around disability based on the medical model. (Oliver, 1990).

In this report, the Medical and Social Models of disability are explained, the relevance of both and their importance in society. My own personal views on both are contained throughout and within the conclusion, based on research, referenced and listed in the bibliography.